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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6829 |
EPI-001
EPI001,EPI 001 |
Apoptosis; Androgen Receptor; PPAR | Apoptosis; DNA Damage/DNA Repair; Endocrinology/Hormones; Metabolism |
EPI-001 是一种选择性雄激素受体 (AR) 的抑制剂,靶向 AR 的反式激活单元 5,可抑制 AR 氨基末端结构域的反式激活,IC50值约为 6 μM。它也是一种选择性的PPARγ调节剂,对去势抵抗性前列腺癌具有活性。 | |||
TP1031 |
Tetracosactide
Tetracosactrin,替可克肽 |
Others | Others |
Tetracosactide (Tetracosactrin) 是一种肾上腺皮质激素 (ACTH) 的类似物,能够刺激肾上腺皮质激素分泌。 | |||
T5885 |
N-Acetyl-D-galactosamine
GalNAc,2-乙酰胺基-2-脱氧-D-半乳糖 |
Others | Others |
N-Acetyl-D-galactosamine (GalNAc) 是一种源自半乳糖的末端必需氨基糖,在人体中形成 A 型血的抗原。 | |||
T40026 |
Butanoic acid, 4-[[2-(2,6-dioxo-3-piperidinyl)-2,3-dihydro-1,3-dioxo-1H-isoindol-4-yl]amino]-
4-[[2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindol-4-yl]amino]butanoic acid |
Others | Others |
Butanoic acid, 4-[[2-(2,6-dioxo-3-piperidinyl)-2,3-dihydro-1,3-dioxo-1H-isoindol-4-yl]amino]- (4-[[2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindol-4-yl]amino]butanoic acid)可用于后续化学的带有烷基接头和末端酸的 Cereblon 配体。 | |||
TP1153L |
Fibronectin Adhesion-promoting Peptide acetate
Fibronectin Adhesion-promoting Peptide acetate(125720-21-0 free base),Heparin Binding Peptide acetate |
Others | Others |
Fibronectin Adhesion-promoting Peptide acetate (Heparin Binding Peptide acetate)(125720-21-0 free base) 是在纤连蛋白的羧基末端肝素结合结构域中发现的肝素结合氨基酸序列之一。 | |||
TP1315 |
c-Myc Peptide Trifluoroacetate
|
Others | Others |
c-Myc Peptide Trifluoroacetate (145646-22-6 free base) 是一种合成肽,对应于人类 c-myc 蛋白的 C 末端氨基酸 (410-419),参与调控生长相关基因的转录。 | |||
TP1615L |
IKKγ NBD Inhibitory Peptide acetate
IKKγ NBD Inhibitory Peptide acetate(372146-18-4 free base) |
NF-κB | NF-κB |
IKKγ NBD Inhibitory Peptide acetate 是一种 NEMO 结合结构域肽(NBD 肽)乙酸盐,对应于 NEMO 氨基末端 α-螺旋区域。它显示可阻断 TNF-α 诱导的 NF-kB 活化。 | |||
TP1197 |
Sincalide
SQ19844,辛卡利特,CCK-8,Cholecystokinin octapeptide |
Others | Others |
Sincalide (CCK-8) 是一种速效的胆囊收缩素的氨基酸多肽激素类似物,可在胆囊造影术中静脉使用。它的肝胆生理作用是增加胆汁的分泌,使胆囊收缩并使 Oddi 的括约肌松弛,从而使胆汁排入十二指肠。它是一种通过注射促进胆囊收缩并帮助诊断胆囊和胰腺疾病的药物。 | |||
TP1280 |
Hexa-His
|
Others | Others |
Hexa-His 是融合蛋白的金属结合位点,是一种由 6 个组氨酸构成的六肽。 | |||
T9417L |
gamma-preprotachykinin amide (72-92) acetate
gamma-preprotachykinin amide (72-92) acetate (114882-65-4 Free base) |
Others | Others |
gamma-preprotachykinin amide (72-92) acetate 是一种 21 个氨基酸的肽,属于速激肽 (TK) 家族,在其 C 末端序列中包括神经激肽 A (NKA)。它对中枢 NK-2 受体的亲和力高于 NKA;它对 NK-1 受体的亲和力较低,但是,它有效地刺激唾液分泌,这是由 NK-1 受体激活介导的。 | |||
TP1604L |
Thioredoxin reductase peptide acetate
Thioredoxin reductase peptide acetate(950890-23-0 free base) |
Others | Others |
Thioredoxin reductase peptide acetate(950890-23-0 free base) 对应于硫氧还蛋白还原酶 (TrxR) 中的 53–67 位残基,用于硫氧还蛋白还原酶研究。哺乳动物硫氧还蛋白还原酶 (TR) 催化硫氧还蛋白 (Trx) 的氧化还原活性二硫键的还原,并且在结构和谷胱甘肽还原酶的作用机制,除了 C 末端的 16 个氨基酸延伸部分含有一个罕见的连位硒硫键。 | |||
T32126 |
Hypusine
|
||
Hypusine is an N-terminal amino alcohol derivative of Lys occurring in bovine brain & | |||
T25371 |
Emd 55450
Emd55450,Emd-55450 |
||
Emd 55450 is a synthetic renin antagonist. It is an analog of EMD 55068 with terminal amino group blocked by benzyloxycarbonyl group. | |||
TP1136 |
Secretin (28-54), human
Human secretin |
||
Secretin (28-54), human, is a 27-amino acid residue peptide with a C-terminal amidation, acting on human secretin receptors. | |||
T16173 |
N-(Amino-PEG5)-N-bis(PEG4-acid)
|
Others | Others |
N-(Amino-PEG5)-N-bis(PEG4-acid) is a PEG-based PROTAC linker employed for synthesizing PROTACs. It comprises an amino group with two terminal carboxylic acids[1]. | |||
T37128 |
Chemerin-9, Mouse
|
||
Chemokine-like receptor 1 (CMKLR1) agonist (EC50 = 42 nM). Corresponds to C-terminal of full length mouse Chemerin, amino acids 148 - 156. | |||
T71920 |
9-(Boc-amino)nonanoic Acid
|
||
9-(Boc-amino)nonanoic Acid is an alkane chain with terminal carboxlic acid and Boc-protected amino groups. The compound can be used as a PROTAC linker in the synthesis of PROTACs. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. The Boc group can be deprotected under mild acidic conditions to form the free amine. | |||
T76102 | Carboxypeptidase B | ||
Carboxypeptidase B 是一种肽链外切酶,可专一性地降解肽链。Carboxypeptidase B 从 C 端逐个降解,释放出游离氨基酸。Carboxypeptidase B 只水解以碱性氨基酸(如精氨酸和赖氨酸)为 C 末端残基的肽键。 | |||
T70057 |
14-(Fmoc-amino)-tetradecanoic acid
|
||
14-(Fmoc-amino)-tetradecanoic acid can be used as a PROTAC linker in the synthesis of PROTACs. 14-(Fmoc-amino)-tetradecanoic acid is an alkane chian with terminal Fmoc-protected amine and carboxylic acid groups. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. | |||
TP1547 |
Caerulein, desulfated
|
||
Caerulein, desulfated is the desulfurated form of Caerulein. Caerulein is a deceptide with the same five carboxy-terminal amino acids as gastrin and cholecystatin (CCK). | |||
TP1827 |
Neuronostatin-13 (human)
Neuronostatin-13 human |
||
Neuronostatin-13 (Human) is a 13 amino acid residue peptide with carboxyl-terminal amidation, the primary structure is conserved in human chimpanzee and some other mammals. | |||
TP1153 |
Fibronectin Adhesion-promoting Peptide
Heparin Binding Peptide |
||
Fibronectin Adhesion-promoting Peptide (Heparin Binding Peptide) is one of the heparin-binding amino acid sequences found in the carboxy-terminal heparin-binding domain of fibronectin. | |||
TP1448 |
Astressin
|
||
Astressin is an amino-terminal truncated analog of CRF that retains high affinity binding to the extracellular domain of the receptor and is believed to act as a neutral competitive antagonist of receptor activation. | |||
T71906 |
Boc-12-Ado-OH
|
||
Boc-12-Ado-OH can be used as a PROTAC linker in the synthesis of PROTACs. Boc-12-Ado-OH is an alkane chain with terminal carboxlic acid and Boc-protected amino groups. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. The Boc group can be deprotected under mild acidic conditions to form the free amine. | |||
TP1645 |
β-Amyloid (1-9)
β-Amyloid 1-9 |
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This is an N-terminal fragment of beta amyloid. It consists of amino acid residues 1 to 9. Truncated beta amyloid peptide (10-40) still forms amyloid fibrils and shows fibril polymorphism. | |||
T71872 | Boc-8-aoc-oh | ||
Boc-8-aoc-oh can be used as a PROTAC linker in the synthesis of PROTACs. Boc-8-aoc-oh is an alkane chain with terminal carboxlic acid and Boc-protected amino groups. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. The Boc group can be deprotected under mild acidic conditions to form the free amine. | |||
T70303 | N-Boc-15-aminopentadecanoic acid | ||
N-Boc-15-aminopentadecanoic acid is an alkane chain with terminal carboxlic acid and Boc-protected amino groups. The compound can be used as a PROTAC linker in the synthesis of PROTACs. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. The Boc group can be deprotected under mild acidic conditions to form the free amine. | |||
T71789 | Boc-7-Aminoheptanoic acid | ||
Boc-7-Aminoheptanoic acid can be used as a PROTAC linker in the synthesis of PROTACs and other conjugation applicaitons. Boc-7-Aminoheptanoic acid is an alkane chain with terminal carboxlic acid and Boc-protected amino groups. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. The Boc group can be deprotected under mild acidic conditions to form the free amine. | |||
T71970 |
Fmoc-7-amino-heptanoic acid
|
||
Fmoc-7-amino-heptanoic acid is an alkane chian with terminal Fmoc-protected amine and carboxylic acid groups. The compound can be used as a PROTAC linker in the synthesis of PROTACs. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. | |||
T76459 |
[Tyr12] Somatostatin 28 (1-14)
|
||
[Tyr12] Somatostatin 28 (1-14),是Somatostatin-28 (1-14)的类似物,属于神经肽生长抑素-28的N-末端片段。 | |||
T71919 |
Boc-10-Aminodecanoic acid
|
||
Boc-10-Aminodecanoic acid can be used as a PROTAC linker in the synthesis of PROTACs and other conjugation applications. Boc-10-Aminodecanoic acid is an alkane chain with terminal carboxlic acid and Boc-protected amino groups. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. The Boc group can be deprotected under mild acidic conditions to form the free amine. | |||
TP1152 |
Fibronectin Adhesion-promoting Peptide TFA
Heparin Binding Peptide TFA |
||
Fibronectin Adhesion-promoting Peptide (Heparin Binding Peptide) is one of the heparin-binding amino acid sequences found in the carboxy-terminal heparin-binding domain of fibronectin. It promotes assembly of mesenchymal stem cell (MSC) spheroids into lar | |||
T83115 | Angiogenin Fragment (108-123) | ||
Angiogenin Fragment (108-123) 为血管生成素C末端的第108至123氨基酸片段,具有抑制其酶促活性和生物活性的功能。 | |||
TP1576 |
SNAP-25 187-203
|
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This amino acids187 to 203 fragment is derived from the C-terminal helix of synaptosomal-associated protein of 25 kDa (SNAP-25). This peptide is able to rescue exocytosis from botulinum neurotoxin E (BoNT/E)-treated cells, albeit at higher concentrations | |||
TP1032 |
Transdermal Peptide TFA (918629-48-8 free base)
Transdermal Peptide TFA,TD 1 (peptide) (TFA) |
||
Transdermal Peptide TFA (TD 1 Peptide TFA) is an 11-amino acid polypeptide that binds to Na+/K+ -atpase beta-subunit (ATP1B1) and interacts with the C terminal of ATP1B1.Transdermal Peptide TFA can enhance the transmission of some large molecules in the s | |||
TP2177 |
Amyloid Precursor C-Terminal Peptide
|
Others | Others |
Amyloid precursor c-terminal peptide has the amino acid sequence Gly-Tyr-Glu-Asn-Pro-Thr-Tyr-Lys-Phe-Phe-Glu-Gln-Met-Gln-Asn. APP is best known as the precursor molecule whose proteolysis generates beta-amyloid (Aβ), a 37 to 49 amino acid peptide whose am | |||
TP1615 |
IKKγ NBD Inhibitory Peptide
|
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A cell-permeable synthetic peptide NEMO-binding domain peptide (NBD peptide) corresponding to the NEMO amino-terminal alpha-helical region is shown to block TNF-alpha-induced NF-kB activation. The interaction of IKγNEMO with the IKK complex is vital for t | |||
TP1514 |
α-Neoendorphin (1-8)
α-Neoendorphin 1-8 |
||
α-Neoendorphin (1-8) is a 8-amino acid peptide derived from the N-terminal of α-Neoendorphin. α-Neoendorphin is an endogenous opioid peptide and is a part for the neoendorphins which are a group of endogenous opioid peptides derived from the proteolytic c | |||
T76202 | Recombinant Proteinase K | ||
Recombinant Proteinase K为一种serine protease,专门裂解脂肪族及芳香族氨基酸的羧基端肽键,适用于蛋白质消化与清除核酸制剂中的污染。 | |||
T81585 |
Oxyntomodulin (human, mouse, rat)
Proglucagon (33-69) |
||
Oxyntomodulin (human, mouse, rat) (Proglucagon (33-69)) 是由胰高血糖素前体产生,融合了完整胰高血糖素序列和C端八肽,含37个氨基酸。 | |||
T76308 |
Gastric Inhibitory Polypeptide (1-30), porcine
|
||
Gastric Inhibitory Polypeptide (1-30), porcine 缺乏天然胃抑制多肽 (GIP) C 端 12 个氨基酸残基,能够增强胰岛素和生长抑素的释放而发挥生物活性。 | |||
T36876 | SBP1 | ||
Human ACE2 receptor-derived 23-amino acid peptide. Binds receptor binding domain (RBD) of insect-derived SARS-CoV-2 spike protein (KD = 1.3 μM for N-terminal biotinylated, insect-derived spike protein RBD; see Zhang et al preprint publication). Please note - unpublished, in-house data suggests approximately 75-fold lower affinity for insect-derived SARS-CoV-2 RBD than reported by Zhang et al. | |||
TP1130 |
β-CGRP, human
CGRP-II (Human),Human β-CGRP |
||
β-CGRP, human ,a 37-amino acid peptide,is the beta form of Calcitonin-gene-related peptide (β-CGRP), involved extensively in regulation of the cardiovascular and nervous systems. β-CGRP contains a disulphide bridge at the N-terminus, a C-terminal phenylal | |||
TP1944 |
pep2-SVKI
|
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Inhibitor peptide corresponding to last 10 amino acids of the C-terminus of the GluA2 AMPA receptor subunit. Disrupts binding of GluA2 (at the C-terminal PDZ site) with glutamate receptor interacting protein (GRIP), AMPA receptor binding protein (ABP) and | |||
T35827 |
Epsilon-V1-2
PKCε Inhibitor Peptide,Protein Kinase Cɛ Inhibitor Peptide,ɛV1-2 |
||
Protein kinase C (PKC ) is a calcium-independent, phospholipid- and diacylglycerol-dependent serine/threonine kinase involved in diverse signaling pathways, including those involved in neuronal signaling, cytoskeletal function, and inflammation.[1] PKC inhibitor peptide is a synthetic peptide corresponding to an amino acid sequence found in the amino terminal C2 domain of most mammalian forms of PKC .[2] It selectively and reversibly inhibits the translocation of PKC to intracellular membrane... | |||
T83221 |
a-Bag Cell Peptide (1-7)
|
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α-Bag Cell Peptide (1-7)是α-bag cell peptide的NH2末端片段,具有抑制左上象限(LUQ)神经元及阻止袋细胞去极化的功能。 | |||
T80228 |
r8-Gly-Noxa A BH3
|
||
r8-Gly-Noxa A BH3 是一种源自 Noxa A BH3 (死亡结构域) 结构域氨基酸残基 17 至 36 的具有生物活性的细胞渗透性肽。该肽在氨基末端通过添加 8 个 D-精氨酸残基和一个甘氨酸接头残基而进行了修饰。 | |||
T77087 | Mipeginterferon alfa-2b | ||
Mipeginterferon alfa-2b 是一种干扰素IFNA2b 类似物。包括一个 N 末端和 10 个赖氨酸 N6 在内的 11 个氨基,平均被取代掉 5 个。Mipeginterferon alfa-2b 的相对分子质量为 40 kDa。 | |||
T76168 |
Carboxypeptidase C
|
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CarboxypeptidaseC为生化研究中常用的羧肽酶,专门用于切除多肽链羧基末端的赖氨酸、精氨酸和脯氨酸,同时也能处理包含中性、脂肪族、芳香族及酸性蛋白质氨基酸的肽链。 | |||
T76376 |
Lys-Gln-Ala-Gly-Asp-Val
|
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Lys-Gln-Ala-Gly-Asp-Val (KQAGDV), 纤维蛋白原γ链(fibrinogen γ-chain)末端六个氨基酸组成,是细胞粘附肽。通过α2bβ3整合素,介导细胞粘附,对平滑肌细胞(SMCs)具有有效粘附配体功能。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4757 |
L-Homoserine
(S)-2-氨基-4-羟基丁酸,(S)-(-)-2-AMINO-4-HYDROXYBUTYRIC ACID |
Others; Endogenous Metabolite | Metabolism; Others |
L-Homoserine ((S)-(-)-2-AMINO-4-HYDROXYBUTYRIC ACID) 是天然存在的非蛋白丝氨酸,是合成苏氨酸、蛋氨酸和赖氨酸的共有中间体。它是氨基酸丝氨酸的更具反应性的变体。 | |||
T4889 |
2,6-Diaminoheptanedioic acid
|
Others; Endogenous Metabolite | Metabolism; Others |
2,6-Diaminoheptanedioic acid 是内源性代谢产物的一种。 |